| ²é¿´: 355 | »Ø¸´: 2 | ||
wangcong123ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
¹þ¹þ
|
[ÇóÖú]
»¯ºÏÎï½âÆ×--- ̼Æ× ÒÑÓÐ1È˲ÎÓë
|
| ÒÔÏÂΪ»¯ºÏÎïµÄ̼Æ×£¬13C NMR (126 MHz, dmso) ¦Ä 176.74, 154.01, 138.63, 134.04, 127.62, 122.34, 120.25, 107.79, 107.32.¡£·Ö×ÓÁ¿Îª295 |
» ±¾ÌûÒÑ»ñµÃµÄºì»¨£¨×îÐÂ10¶ä£©
» ²ÂÄãϲ»¶
0703×Ü·Ö331Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
085600£¬321·ÖÇóµ÷¼Á
ÒѾÓÐ7È˻ظ´
325Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
085600£¬320·ÖÇóµ÷¼Á
ÒѾÓÐ12È˻ظ´
Ò»Ö¾Ô¸0817»¯Ñ§¹¤³ÌÓë¼¼Êõ£¬Çóµ÷¼Á
ÒѾÓÐ27È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤085600 310·ÖÇóµ÷¼Á
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸¹þ¶û±õ¹¤Òµ´óѧ085600Ó¢Ò»Êý¶þ337·ÖÇóµ÷¼Á
ÒѾÓÐ10È˻ظ´
22408Çóµ÷¼Á 354·Ö ¿É¿çרҵ
ÒѾÓÐ3È˻ظ´
277¹¤¿ÆÇóµ÷¼Á
ÒѾÓÐ4È˻ظ´
Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á£¬326·Ö
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹ØÉ̼ÒÍÆ¼ö: (ÎÒÒ²ÒªÔÚÕâÀïÍÆ¹ã)
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÈýÝÆ»¯ºÏÎï̼Æ×´óÈ«
ÒѾÓÐ6È˻ظ´
½âÆ×ÇóÖú£¨Ö»ÓÐ̼Æ×£©£¬Ð»Ð»ÁË¡£
ÒѾÓÐ3È˻ظ´
Ç×°®µÄ³æÓÑÃÇ ¹òÇó½âÆ×(̼Æ× ÇâÆ× ÖÊÆ×£© ¼±
ÒѾÓÐ19È˻ظ´
MestReNova HMBC ÇâÆ×¼°Ïà¹Ø²»È«
ÒѾÓÐ4È˻ظ´
ÊÇ·ñ´æÔÚÁ½ÖÖ»¯ºÏÎïÇâÆ×̼Æ×Ò»Ñù£¬µ«ÊÇdept-135ºÍdept-90µÄͼÊÇÕýºÃÏà·´µÄ£¿
ÒѾÓÐ6È˻ظ´
΢Æ×ÇóÖú1¸ö»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
Õâ¸ö»¯ºÏÎï´¿Â𣿻¹ÐèÒª´ò̼Æ×»¹ÊÇÔÙÖÆ±¸¡£ÓÃÀ´¿´DMSO
ÒѾÓÐ7È˻ظ´
»¯ºÏÎï×öH-NMRÆ×º¬µãÔÓÖÊÄܲ»ÄÜ×ö
ÒѾÓÐ6È˻ظ´
ÇóÖúÈý¸ö»¯ºÏÎ̼Æ×£©µÄ΢Æ×Êý¾Ý¿â¼ìË÷½á¹û£¨ÏàËÆ¶Èǰ20%£©
ÒѾÓÐ3È˻ظ´
Á½¸öÈýÝÆÀ໯ºÏÎï΢Æ×̼Æ×Êý¾Ý²éѯ
ÒѾÓÐ9È˻ظ´
MESTRENOVA 7 ½â̼Æ×£¬ÈçºÎÈÃÊä³öµÄÊý¾Ý±£ÁôһλСÊý£¨Ä¬ÈÏÊÇÁ½Î»£©£¿
ÒѾÓÐ12È˻ظ´
¼òµ¥»¯ºÏÎï½âÆ× 6»ò8¸ö̼ £¡£¡£¡£¡ 7¸öÇâ
ÒѾÓÐ24È˻ظ´
ºË´Å̼Æ×»¯Ñ§Î»ÒÆÌصã
ÒѾÓÐ7È˻ظ´
ÇóÖú½âÎöÒ»»¯ºÏÎïµÄHÆ×CÆ×£¬¸½ÉÏͼÆ×
ÒѾÓÐ13È˻ظ´
¡¾ÇóÖú¡¿·ÖÀëÌá´¿µÃµ½µÄ»¯ºÏÎï¼òµ¥ÇâÆ×ºÍ̼Æ×½âÎö
ÒѾÓÐ10È˻ظ´
Ïõ»ùßäßò»¯ºÏÎïÇâÆ×̼Æ×ÇóÖú
ÒѾÓÐ7È˻ظ´
¹ØÓÚ»¯ºÏÎï̼Æ×»¯Ñ§Î»ÒƶԲ»ÉÏ£¬ÐèУÕýµÄÎÊÌâ¡£Çó¸ßÈ˽â´ð...
ÒѾÓÐ8È˻ظ´
Çó¸ßÊÖÖ¸µã£º»¯ºÏÎïÄÜ×ö³ö1HNMR ºÍ MSµ«ÊÇ×ö²»³ö̼Æ× ÕâÊÇΪºÎ£¿
ÒѾÓÐ9È˻ظ´
¡¾ÇóÖú¡¿Çë³æÓÑÃǰï°ï½âÒ»ÏÂÕâ¸ö»¯ºÏÎï°¡£¬ÓÐÇâÆ×£¬Ì¼Æ×ºÍÖÊÆ×Êý¾Ý
ÒѾÓÐ9È˻ظ´
¡¾ÇóÖú¡¿ÇóÖú½âÆ×CÆ×ºÍHÆ×
ÒѾÓÐ22È˻ظ´
¡¾ÇóÖú¡¿¡¾ÇóÖú¡¿·ÖÀëÌá´¿µÄ»¯ºÏÎï¼òµ¥ÇâÆ×ºÍ̼Æ×½âÎö
ÒѾÓÐ15È˻ظ´
¡¾ÇóÖú¡¿±£Áôʱ¼ä²»Ò»ÑùµÄÁ½¸ö»¯ºÏÎïµÄÇâÆ×̼Æ×Ò»Ñù£¿
ÒѾÓÐ13È˻ظ´
¡¾ÇóÖú¡¿ë®´ø»¯ºÏÎï̼Æ× Çó½âÊÍ
ÒѾÓÐ10È˻ظ´
¡¾ÇóÖú¡¿ËÖªµÀÄÄÀï¿ÉÒԲ黯ºÏÎïµÄ̼Æ×°¡£¿
ÒѾÓÐ10È˻ظ´

wangcong123
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
¹þ¹þ
- Ó¦Öú: 9 (Ó×¶ùÔ°)
- ½ð±Ò: 20784.7
- ºì»¨: 9
- Ìû×Ó: 4347
- ÔÚÏß: 213.8Сʱ
- ³æºÅ: 1403295
- ×¢²á: 2011-09-15
- ÐÔ±ð: GG
- רҵ: º£ÑóÒ©Îï

2Â¥2014-12-09 16:52:56
·çÐÐÕß007
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1309 (½²Ê¦)
- ½ð±Ò: 12672.8
- ºì»¨: 15
- Ìû×Ó: 1490
- ÔÚÏß: 299.5Сʱ
- ³æºÅ: 2542465
- ×¢²á: 2013-07-12
- ÐÔ±ð: GG
- רҵ: ÓлúºÏ³É
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
|
²éѯ½á¹û£º¹²²éµ½52¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 6-hydroxykynurenic acid ÏàËÆ¶È:70% Planta Medica 1988 54 245-247 Isolation of Flavonol Glycosides from Ginkgo biloba Leaves C. VCtoffe, M. Haag-Berrurier, A. Lobstein-Guth, J. P. Balz, and R. Anton Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 6-hydroxykynurenic acid ÏàËÆ¶È:70% Korean Journal of Pharmacognosy 1995 26(1) 23-26 Phytochemical Analysis of Ginkgo biloba Yellow Leaves Kang, Sam-Sik; Koh, Young-Min; Kim, Ju-Sun; Lee, Myung-Whan; Lee, Dong-Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 7-hydroxy-1-oxo-1,2-dihydroisoquinoline-5-carboxylic acid C10H7NO4 ÏàËÆ¶È:60% Journal of Natural Products 2008 71(6) 1092-1094 (Iso)-Quinoline Alkaloids from Fungal Fruiting Bodies of Cortinarius subtortus Axel Teichert, Ju#rgen Schmidt, Andrea Porzel, Norbert Arnold, and Ludger Wessjohann Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . indole-2-carbaldehyde thiocarbohydrazone C10H11N5S ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2013 69 144-150 Synthesis of Novel Indole Hydrazone Derivatives and Evaluation of Their Antiplatelet Aggregation Activity Vida Mashayekhi, Kamaleddin Haj Mohammad Ebrahim Tehrani, Salimeh Amidi, Farzad Kobarfard Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Compound 1 ÏàËÆ¶È:55.5% Tetrahedron Letters 2012 53 509-513 Palladium-catalysed direct arylations of NH-free pyrrole and N-tosylpyrrole with aryl bromides Charles Beromeo Bheeter,Jitendra K. Bera,Henri Doucet Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 2-amino-1-methylimidazo[4,5-b]thieno[3,2-e] pyridine C9H8N4S ÏàËÆ¶È:55.5% Heterocycles 2005 65 2369-2380 Synthesis of Thienoimidazo[4,5-b]pyridines and Thenylidenoimidazolinones Malin Björk and Spiros Grivas* Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Compound 5 ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry Letters 2001 11 191-193 High-pressure synthesis of enantiomerically pure C-6 substituted pyrazolo[3,4-d]pyrimidines Sally-Ann Poulsen, David J. Young, Ronald J. Quinn Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Compound 2 ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry Letters 1996 6 1901-1904 Synthesis, characterization, and anti-HIV activity of some 2-p-X-phenyl-1,3-N,N'-diphenyl-amidines Aurea Echevarria, Lucia Helena Santos, Joseph Miller, Naheed Mahmood Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Compound 3 ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry Letters 1996 6 1901-1904 Synthesis, characterization, and anti-HIV activity of some 2-p-X-phenyl-1,3-N,N'-diphenyl-amidines Aurea Echevarria, Lucia Helena Santos, Joseph Miller, Naheed Mahmood Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 3,5-di(4-hydroxy-3-nitrophenyl)pyridine ÏàËÆ¶È:55.5% Tetrahedron Letters 2005 46 6457-6460 Remarkable Chichibabin-type cyclotrimerisation of 3-nitrotyrosine, tyrosine and phenylalanine to 3,5-diphenylpyridine derivatives induced by hypochlorous acid L. Panzella, P. Di Donato, S. Comes, A. Napolitano, A. Palumbo, M. d¡¯Ischia Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 4,4'-bis-(3-methyl-1H-imidazolium-1-yl)biphenyldiiodide C20H20N4I2 ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry 2011 19 6525-6542 The anti-malarial activity of bivalent imidazolium salts Jason Z. Vlahakis, Simona Mitu, Gheorghe Roman, E. Patricia Rodriguez, Ian E. Crandall, Walter A. Szarek Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . bis(1H-indol-2-yl)selenide C16H12N2Se ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry 2009 17 1648-1653 Synthesis and biological evaluation of fused thio- and selenopyrans as new indolocarbazole analogues with aryl hydrocarbon receptor affinity Emma Wincent, Hamid Shirani, Jan Bergman, Ulf Rannug, Tomasz Janosik Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . bis(5-methoxy-1H-indol-2-yl)selenide C18H16N2O2S ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry 2009 17 1648-1653 Synthesis and biological evaluation of fused thio- and selenopyrans as new indolocarbazole analogues with aryl hydrocarbon receptor affinity Emma Wincent, Hamid Shirani, Jan Bergman, Ulf Rannug, Tomasz Janosik Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 5-chloroindole-2-carbonyl chloride C22H15ClN2O2 ÏàËÆ¶È:55.5% Molecules 2011 16 8292-8304 Antihyperlipidemic Properties of Novel N-(Benzoylphenyl)-5-substituted-1H-indole-2-carboxamides in Triton WR-1339-Induced Hyperlipidemic Rats Yusuf Al-Hiari, Ghassan Shattat, Tariq Al-Qirim, Waseem El-Huneidi, Ghassan Abu Sheikha and Suhair Hikmat Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 4-(4-pyridyl)-2-nitroaniline C11H9N3O2 ÏàËÆ¶È:55.5% Journal of Medicinal Chemistry 1995 38 3638-3644 Synthesis and Evaluation of Terbenzimidazoles as Topoisomerase I Inhibitors Qun Sun, Barbara Gatto, Chiang Yu, Angela Liu, Leroy F. Liu, Edmond J. LaVoie Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . cis-bis(3-hydroxy-2-methyl-1-phenyl-4-pyridinonato)dioxomolybdenum(VI) C24H20N2 ÏàËÆ¶È:55.5% Canadian Journal of Chemistry 1999 77 1249-1261 Synthesis, characterization, and biological relevance of hydroxypyrone and hydroxypyridinone complexes of molybdenum Sarah J. Lord, Noah A. Epstein, Robert L. Paddock, Christopher M. Vogels,Tracy L. Hennigar, Michael J. Zaworotko, Nicholas J. Taylor,William R. Driedzic, Tom L. Broderick, and Stephen A. Westcott Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 5-chloroindole-3-carboxylic acid C9H6ClNO2 ÏàËÆ¶È:55.5% Natural Product Research 2013 27 1366-1371 A new 20-membered macrolide produced by a marine-derived Micromonospora strain Peng Fei, Wang Chuan-xi, Xie Yang, Jiang Hong-lei, Chen Lu-jie, Paulina Uribe, Alan T. Bull, Michael Goodfellow, Jiang Hong & Lian Yun-yang Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 3-amino-1H-isoindol-1-one thiosemicarbazone C9H9N5S ÏàËÆ¶È:55.5% Journal of Heterocyclic Chemistry 2013 50 1140-1145 A One-Pot Synthesis of 3-Amino-1H-isoindol-1-one thiazol-2-ylhydrazones Angelina Biitseva, Ulrich Groth and Olga Hordiyenko Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . compound 9 ÏàËÆ¶È:55.5% Magnetic Resonance in Chemistry 1990 28 807-811 1H and 13C NMR study of the structure of pyrazoles, imidazoles and their benzo derivatives in sulphuric acid (azolium cations) Jos¨¦ Elguero, Mar¨ªa Luisa Jimeno and Gloria I. Yranzo Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . saccharin ÏàËÆ¶È:55.5% Organic Magnetic Resonance 1983 21 187-189 13C NMR spectra of benzothiazepinone, benzothiazinone and benzosulphonamide N-substituted derivatives C. I. Stassinopoulou, P. Catsoulacos and Ch. Camoutsis Structure 13C NMR ̼Æ×Ä£Äâͼ |

3Â¥2014-12-09 17:15:42














»Ø¸´´ËÂ¥
wangcong123